Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 19 and up

Influenza Vaccine Immunogenicity in Older Adults with Repeated Vaccination

Official title: Immunogenicity of Different Influenza Vaccine Strategies in Older Adults in a Repeated Vaccination Setting

Run by Korea University Guro Hospital · NCT07838298 · Data updated 2026-11-12

This study tests how different flu vaccines perform in adults 65+ who get yearly vaccines to see if age and repeated vaccination affect the immune response.

More Older Adults (65 Years and Older) trials

Quick facts

PhasePhase 4
Study typeInterventional
Ages19 Years and up
SexAll
Enrollment180 (estimated)
SponsorKorea University Guro Hospital
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Seoul)
StatusRecruiting
StartedSeptember 21, 2026
Main results expectedDecember 2028
Study endsDecember 2028
Registry record updatedSeptember 24, 2026
Trial IDNCT07838298 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 65 or older who plan to receive annual influenza vaccination and can complete follow-up visits.

Probably not a fit

Patients with recent influenza vaccination, immunocompromising conditions, or contraindications to vaccination may not experience a clear benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This Phase 4 trial compares three influenza vaccine formulations—standard dose, MF59 adjuvanted, and high dose—in adults 65 years and older. A younger reference group (19–49 years) receiving standard-dose vaccine helps contextualize age-related differences. Participants will receive a vaccine and provide blood samples to measure immune responses over time. The study aims to understand how immune aging and repeated vaccination influence immunogenicity across formulations. Exclusion criteria include recent vaccination, immunocompromising conditions, and any contraindication to vaccination.

Why it matters

Potential benefit: If successful, the study could clarify which vaccine formulation offers stronger immune responses in older adults who are repeatedly vaccinated.

How similar studies have gone: Previous studies have explored vaccine immunogenicity in older adults, with mixed results across formulations, making this approach informative but not entirely novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Older adult group: aged 65 years or older
* Younger reference group: aged 19 to 49 years
* Able to receive influenza vaccination and complete the scheduled follow up

Exclusion Criteria:

* Receipt of an influenza vaccine or any other vaccine within 4 weeks prior to enrollment
* Immunocompromised status, including ongoing chemotherapy or immunosuppressive therapy, high dose corticosteroid therapy, history of solid organ or hematopoietic stem cell transplantation, active malignancy, HIV infection, or other clinically significant immunocompromising conditions
* Moderate or severe acute infection
* History of allergic reaction to an influenza vaccine or any of its components, or any other condition that precludes influenza vaccination
* Inability, as determined by the investigator, to understand the purpose and procedures of the study and provide voluntary informed consent

Where it's running

  • Korea University Guro Hospital
    Seoul, South Korea
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.